Canonical Allele Identifier: CA1458424537
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.54072448C= , CM000666.2:g.54072448C= GRCh38
NC_000004.11:g.54938615C= , CM000666.1:g.54938615C= GRCh37
NC_000004.10:g.54633372C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000507166.5:c.1018-202477C= ENSP00000423325.1:n.1018-202477C=